Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
` QM 34458
33730~
AQUEOUS DISPERSIONS
This invention relates to aqueous dispersions and
more particularly to aqueous polymer dispersions
containing a water-dispersible polyurethane and a vinyl
polymer.
Aqueous polyurethane dispersions are well known
and are used in the production of, for example, coatings
and films, Aqueous dispersions are also known which
contain a dispersed vinyl polymer in addition to a
polyurethane.
Thus, U.S.Pat. No. 3862074 describes coating or
binding compositions which are aqueous emulsions or
dispersions of one or more acrylic polymers and one or
more urethane polymers, the product being prepared by
simply blending a nonionic urethane dispersion and an
acrylic dispersion. The only polyurethane described is a
reaction product of a diamine and an isocyanate-
terminated prepolymer derived from a polyether polyol and
toluene diisocyanate.
Several patents describe processes wherein the
vinyl monomer is polymerised in the presence of the
aqueous polyurethane dispersion. In U.S. Pat. No.
3705164, the only polyisocyanates mentioned for the
production of the polyurethane are hexamethylene
diisocyanate and toluene diisocyanate. U.S. Pat. No.
4198330 mentions aromatic, aliphatic and cycloaliphatic
diisocyanates but expresses a preference for toluene
diisocyanate. In U.S. Pat. No. 4318833, the preferred
diisocyanates are of the aliphatic type but some aromatic
diisocyanates including toluene and 4,4'-diphenylmethane
disocyanates are mentioned. In EP-A-189945, the
preferred polyisocyanate seems to be dicyclohexylmethane
diisocyanate.
It has now been found that aqueous dispersions
containing a vinyl polymer and a polyurethane derived,
~ 2 - 1 337309
at least in part, from 2,4'-diphenylmethane diisocyanate
possess significant advantages over corresponding
dispersions described in the prior art. Thus,coatings
are obtained which are harder than those obtained from
the corresponding TDI based products and have superior
resistance towards water and a wide range of organic
solvents.
Accordingly, the invention provides an a~ueous
polymer dispersion containing a water-dispersible
polyurethane and a vinyl polymer, the polyurethane being
the product of reacting an active hydrogen containing
chain extender with a water-dispersible
isocyanate-terminated polyurethane prepolymer derived
from a polyisocyanate component containing at least 5% by
weight of 2,4'diphenylmethane diisocyanate.
The isocyanate-terminated prepolymer may owe its
water-dispersibility to the use of external dispersing or
emulsifying agents, for example surface active agents of
a cationic, anionic or nonionic type but it is preferred
that the prepolymer is dispersible because of the
presence therein of appropriate ionic or nonionic
groups.
Water-dispersible isocyanate-terminated
prepolymers containing ionic centres may be the reaction
products of:
(i) a polyisocyanate component containing at least 5%
by weight of 2,4'-diphenylmethane diisocyanate,
and
(ii) an active hydrogen component comprising at least
one polymeric polyol having a molecular weight in
the range 400 to 6000 and optionally one or more
low molecular weight polyol or polyamine having a
molecular weight below 400, at least one of the
polyols or polyamine containing ionic or
potentially ionic groups.
_ 3 1 33730q
The ionic groups may be cationic, for example
-N-, -P- or -S+
or anionic, for example -S3-~ -OS3-~ -P2-~ -P3-~
OP03-, or, preferably -COO~.
The term "potentially ionic" refers to groups such
as free carboxylic acid or tertiary amino groups which
can be converted to ionic groups by neutralisation or
~uaternisation.
In general, anionic groups are preferably
incorporated in the prepolymer in the form of a low
molecular weight polyol or polyamine whilst cationic
groups may be conveniently incorporated by means of
either a polymeric polyol or a low molecular weight
polyol or polyamine.
The polyisocyanate component used in the
preparation of the prepolymer can be mixture of
2,4'diphenylmethane diisocyanate with at least one other
organic polyisocyanate, such mixtures containing at least
5%, preferably at least 10% by weight of the
2,4'-diphenylmethane diisocyanate.
Thus, the polyisocyanate component may be a
mixture of the 2,4'- and the 4,4'-isomers of diphenyl-
methane diisocyanate, possibly with small amounts of the
2,2'-isomer. Such mixtures can contain from 5 to 70% by
weight of the 2,4'-isomer although mixtures containing
more than 70% by weight can also be used.
Other polyisocyanate components which may be used
include carbodiimide/uretonimine modified diphenylmethane
diisocyanates which may be obtained in known manner by
treating a mixture of the 4,4'- and 2,4'-isomers with a
catalyst for the conversion of isocyanate groups to
carbodiimide groups. Suitable catalysts, which include
trialkyl phosphates, phosphoramides, phospholenes and
phospholidines, have been described in United Kingdom
Patent Specification No 1476088.
`:
_ 4 - 1 3373Oq
Further polyisocyanate components which may be
used in the preparation of the prepolymer include
mixtures of any of the above-mentioned diphenylmethane
diisocyanate compositions with other organic
polyisocyanates, especially the commercially available
polyisocyanates such as toluene diisocyanate, isophorone
diisocyanate, hexamethylene diisocyanate and
dicyclohexylmethane diisocyanate. Such mixtures should
contain at least S% by weight of the 2,4'- diphenyl-
methane diisocyanate. Useful mixtures contain toluenediisocyanate, especially an 80/20 mixture of the 2,4- and
2,6-isomers, and one of the above-mentioned
diphenylmethane diisocyanate compositions, especially a
mixture of the 2,4'- and 4,4'-isomers. Thus, a useful
polyisocyanate component comprises:
(i) from 10 to 60% by weight of toluene diisocyanate,
and
(ii) from 90 to 40% by weight of a mixture of 4,4'-
and 2,4'-diphenylmethane diisocyanates containing
from 5 to 70% by weight of the 2,4'-isomer.
Particular mention may be made of mixtures comprising
from 30 to 50% by weight of toluene diisocyanate and
from 70 to 50% by weight of a 4,4'-/2,4'-diphenyl-
methane diisocyanate mixture containing from 10 to 40%,
especially 20 to 30% by weight of the 2,4'-isomer.
Polymeric polyols having molecular weights in the
range 400-6000 which may be used in the preparation of
the prepolymer particularly include diols and triols and
mixtures thereof but higher functionality polyols may be
used, for example as minor components in admixture with
diols. The polyols may be members of any of the chemical
classes of polymeric polyols used or proposed to be used
_ 5 _ 1 33 7 3 09
in polyurethane formulations. In particular, the polyols
may be polyesters, polyesteramides, polyethers,
polythioethers, polycarbonates, polyacetals, polyolefins
or polysiloxanes. Where appropriate, the polyols may
contain free tertiary amino groups. Preferred polyol
molecular weights are from 700 to 2000.
Polyester polyols which may be used include
hydroxyl-terminated reaction products of polyhydric
alcohols such as ethylene glycol, propylene glycol,
diethylene glycol, neopentyl glycol, 1,4-butanediol,
furan dimethanol, cyclohexane dimethanol, glycerol,
trimethylolpropane or pentaerythritol or mixtures
thereof with polycarboxylic acids, especially
dicarboxylic acids or their ester-forming derivatives,
for example succinic, glutaric and adipic acids or their
dimethyl esters, phthalic anhydride or dimethyl
terephthalate. Polyesters obtained by the polymerisation
of lactones, for example caprolactone, in conjunction
with a polyol may also be used. Polyesteramides may be
obtained by the inclusion of amino-alcohols such as
ethanolamine in polyesterification mixtures. Polyesters
containing free tertiary amino groups may be obtained by
including tertiary amino polyols, for example
triethanolamine or N-methyldiethanolamine in the
2S polyesterification reaction.
Polyether polyols which may be used include
products obtained by the polymerisation of a cyclic
oxide, for example ethylene oxide, propylene oxide or
tetrahydrofuran or by the addition of one or more such
oxides to polyfunctional initiators, for example water,
ethylene glycol, propylene glycol, diethylene glycol,
cyclohexane dimethanol, glycerol, trimethylolpropane,
pentaerythritol or Bisphenol A. Especially useful
polyethers include polyoxypropylene diols and triols,
poly(oxyethylene-oxypropylene) diols and triols obtained
- 6 - 1 33 7 309
by the simultaneous or se~uential addition of ethylene
and propylene oxides to appropriate initiators and
polytetramethylene ether glycols obtained by the
polymerisation of tetrahydrofuran. Polyethers containing
free tertiary amino groups may be obtained by the
oxyalkylation, for example oxypropylation, of ammonia,
primary or secondary amines and aminoalcohols. Examples
of suitable amines include ethylene diamine, aniline,
benzylamine, toluene diamines, diaminodiphenylmethane
and polymethylene polyphenyl polyamines. Suitable
aminoalcohols include ethanolamine, diethanolamine,
triethanolamine, N-methyldiethanolamine,
bis(2-hydroxyethyl)aniline, bis(2-hydroxypropyl)aniline
and bis(2-hydroxyethyl)benzylamine. In the oxyalkylation
process, mixtures of amino-containing and amino-free
initiators may be used if desired.
Polythioether polyols which may be used include
products obtained by condensing thiodiglycol either
alone or with other glycols, dicarboxylic acids,
formaldehyde, aminoalcohols or aminocarboxylic acids.
Polycarbonate polyols which may be used include
products obtained by reacting diols such as
1,3-propanediol, 1,4-butanediol, 1,6-hexanediol,
diethylene glycol or tetraethylene glycol with diaryl
carbonates, for example diphenyl carbonate, or with
phosgene.
Polyacetal polyols which may be used include
those prepared by reacting glycols such as diethylene
glycol, triethylene glycol and hexanediol with
formaldehyde. Suitable polyacetals may also be prepared
by polymerising cyclic acetals.
Suitable polyolefin polyols include
hydroxy-terminated butadiene homo- and copolymers.
Organic polyols having molecular weights below
400 which may optionally be used in the preparation of
` _ - 7 - 1337309
the prepolymer particularly include diols and triols and
mixtures thereof but higher functionality polyols may be
used. Examples of such lower molecular weight polyols
include ethylene glycol, diethylene glycol,
tetraethylene glycol, bis(hydroxyethyl) terephthalate,
cyclohexane dimethanol, furan dimethanol, glycerol and
the reaction products, up to molecular weight 399 of
such polyols with propylene oxide and/or ethylene oxide.
Tertiary amino group containing polyols such as
triethanolamine, tetrakis(hydroxypropyl) ethylene diamine
or the lower molecular weight oxyalkylation products of
ammonia, amines and amino-alcohols may be used, for the
purpose of introducing cationic groups into the
prepolymer.
' Low molecular weight polyols or polyamines which
may be used to introduce anionic centres into the
prepolymer include dihydroxyalkanoic acids, for example
2,2-dimethylolpropionic acid and aminocarboxylic acids,
for example lysine, cystine and 3,5-diaminobenzoic acid.
Water-dispersible isocyanate-terminated
prepolymers containing nonionic hydrophilic centres may
be the reaction products of:
(i) a polyisocyanate component containing at least 5%
by weight of 2,4'-diphenylmethane diisocyanate;
(ii) a polymeric polyol having a molecular weight in
the range 400 to 6000;
(iii) a dispersing diol and/or diisocyanate having a
pendent polyoxyethylene chain, and optionally
(iv) an organic polyol having a molecular weight below
400.
Polyisocyanate components, polymeric polyols and
low molecular weight polyols which may be used in
preparing the nonionic prepolymers include those
described above. If desired, the components may be so
~ - 8 - 1 3 3 7 3 0~
chosen that the prepolymers contain both nonionic and
ionic or potentially ionic centres.
Diols having pendent polyoxyethylene chains which
may be used in the preparation of the nonionic prepolymer
S include those described in the prior art, for example in
US 3905929. These diols, because of their function, may
be regarded as dispersing diols. Particularly suitable
dispersing diols may be obtained by reacting one mole of
an organic diisocyanate in which the two isocyanate
groups have different reactivities with approximately one
mole of a polyethylene glycol mono-ether and then
reacting the adduct so obtained with approximately one
mole of a dialkanolamine, for example diethanolamine.
Diisocyanates having groups of different
reactivity which may be used in the preparation of the
dispersing diols include 2,4-toluene diisocyanate,
isophorone diisocyanate and 2,4'-diphenylmethane
diisocyanate. Polyethylene glycol monoethers which may
be used include the reaction products of ethylene oxide
with monohydric alcohols such as methanol, ethanol,
tertiary butanol or benzyl alcohol or phenols such as
phenol itself. The polyethylene glycol monoethers
suitably have molecular weights in the range 250 to 3000
and preferably in the range 500 to 2000.
If desired, the polyoxyethylene chains may
contain units of other alkylene oxides in addition to
the ethylene oxide units. Thus, polyoxyalkylene chains
in which up to 60% of the alkylene oxide units are
propylene oxide units, the remainder being ethylene
oxide units, may be used.
The preparation of the dispersing diols may be
achieved by adding the polyethylene glycol monoether to
the diisocyanate at 20-50C, optionally in the presence
of an inert solvent and a urethane catalyst, followed by
addition of the dialkanolamine.
~ 1 337309
Diisocyanates having pendent polyoxyethylene
chains which may be used in the preparation of the
nonionic prepolymer include those described in the prior
art, for example in US 3920598. These diisocyanates,
because of their function, may be regarded as dispersing
diisocyanates. Particularly suitable dispersing
diisocyanates may be obtained by reacting two moles of an
organic diisocyanate in which the two isocyanate groups
have different reactivities with approximately one mole
of a polyethylene glycol mono-ether, the initially formed
urethane monoisocyanate then reacting at a higher
temperature with the excess diisocyanate to form an
allophanate diisocyanate having a pendent polyoxyethylene
chain.
Suitable diisocyanates and polyethylene glycol
monoethers for use in preparing the dispersing
diisocyanates have been mentioned above for the
preparation of the dispersing diols.
Preferred prepolymers are those in which the
active hydrogen component comprises:
(i) a polymeric diol having a molecular weight of from
400 to 6000, especially from 400 to 1500,
(ii) from 1 to 2 moles, per mole of polymeric diol, of
a carboxy group containing diol or triol, and
(iii) from 0 to 1.2 mole, per mole of polymeric diol, of
a diol having a molecular weight from 62 to 300.
Particularly preferred active hydrogen components
include those in which the polymeric diol is a
polytetramethylene ether glycol, a carboxy-containing
diol, for example dimethylolpropionic acid, is present in
an amount of from 1.2 to 1.6 moles per mole of polymeric
diol and the low molecular weight diol is cyclohexane
dimethanol.
The prepolymers may be prepared in conventional
manner by reacting a stoichiometric excess of the organic
- -10- 133730q
polyisocyanate component with the appropriate active
hydrogen components under substantially anhydrous
conditions at a temperature between about 30C and about
130C until reaction between the isocyanate groups and
the active hydrogen groups is substantially complete. The
polyisocyanate and the active hydrogen containing
components are suitably reacted in such proportions that
the ratio of number of isocyanate groups to the number of
hydroxyl and amino groups is in the range from about
1.1:1 to about 6:1. preferably within the range of from
1.5:1 to 3:1.
If desired, catalysts such as dibutyltin
dilaurate and stannous octoate may be used to assist
prepolymer formation and a non-reactive solvent may be
added before or after prepolymer formation to control
the viscosity. Suitable solvents which may be used
include acetone, methylethylketone, dimethylformamide,
ethylene carbonate, propylene carbonate, diglyme,
N-methylpyrrolidone, ethyl acetate, ethylene and
propylene glycol diacetates, alkyl ethers of ethylene
and propylene glycol monoacetates, toluene, xylene and
sterically hindered alcohols such as t-butanol and
diacetone alcohol. The preferred solvents are
water-miscible solvents such as N-methylpyrrolidone,
dimethyl sulphoxide and dialkyl ethers of glycol acetates
or mixtures of N-methylpyrrolidone and methyl ethyl
ketone. Other suitable solvents include vinyl monomers
which are subsequently polymerised.
Aqueous polyurethane dispersions may be prepared
by dispersing the water dispersible, isocyanate-
terminated polyurethane prepolymer in an aqueous medium
and chain extending the prepolymer with an active
hydrogen containing chain extender.
The prepolymer may be dispersed in water using
technlques well known in the art. Preferably, the
1 337309
prepolymer is added to the water with agitation or,
alternatively, water may be stirred into the prepolymer.
Conversion of any potentially ionic groups, for
example carboxy groups, in the prepolymer to ionic (salt)
groups may be effected before, simultaneously with or
after the addition of the prepolymer to water. The agent
used to effect neutralisation of a carboxy group may
suitably be a tertiary amine such as triethylamine,
triethanolamine or N-methylmorpholine, an alkaline
hydroxide such as sodium or potassium hydroxide or a
quaternary ammonium hydroxde.
The active hydrogen containing chain extender
which is reacted with the prepolymer is suitably a
polyol, an amino alcohol, ammonia, a primary or secondary
aliphatic, alicyclic, aromatic, araliphatic or
heterocyclic amine especially a diamine, hydrazine or a
substituted hydrazine. Water-soluble chain extenders are
preferred, and water itself may be effective.
Examples of suitable chain extenders useful
herein include ethylene diamine, diethylene triamine,
triethylene tetramine, propylene diamine, butylene
diamine, hexamethylene diamine, cyclohexylene diamine,
piperazine, 2-methyl piperazine, phenylene diamine,
tolylene diamine, xylylene diamine, tris(2-aminoethyl)
amine, 3,3'-dinitrobenzidine, 4,4'-methylenebis
(2-chloroaniline), 3,3'-dichloro-4,4'bi-phenyl diamine,
2,6-diaminopyridine, 4,4'-diaminodiphenylmethane,
menthane diamine, m-xylene diamine and isophorone
diamine. Also materials such as hydrazine, azines such
as acetone azine, substituted hydrazines such as, for
example, dimethyl hydrazine,
1,6-hexamethylene-bis-hydrazine, carbodihydrazine,
hydrazides of dicarboxylic acids and sulfonic acids such
as adipic acid mono- or dihydrazide, oxalic acid
~ - 12 - 1 33 73 09
dihydrazide, isophthalic acid dihydrazide, tartaric acid
dihydrazide, l,3-phenylene disulfonic acid dihydrazide,
omega-amino-caproic acid dihydrazide, hydrazides made by
reacting lactones with hydrazine such as
gamma-hydroxylbutyric hydrazide, bis-semi-carbazide,
bis-hydrazide carbonic esters of glycols such as any of
the glycols mentioned above.
Where the chain extender is other than water, for
example a diamine or hydrazine, it may be added to the
aqueous dispersion of prepolymer or, alternatively, it
may already be present in the aqueous medium when the
prepolymer is dispersed therein.
The chain extension can be conducted at elevated,
reduced or ambient temperatures. Convenient
temperatures are from about 5 to 95C or more,
preferably from about 10 to about 45C.
The amount of chain extender employed should be
approximately equivalent to the free-NCO groups in the
prepolymer, the ratio of active hydrogens in the chain
extender to NCO groups in the prepolymer preferably being
in the range from l.0 to 2.0:l. Of course, when water is
employed as the chain extender, these ratios will not be
applicable since the water, functioning both as chain
extender and dispersing medium, will be present in gross
excess relative to the free-NCO groups.
The aqueous polymer dispersion of the invention
may be prepared by simply blending an aqueous
polyurethane dispersion, prepared as described above,
with an aqueous dispersion of a vinyl polymer. It is
preferred, however to polymerise one or more vinyl
monomers in the presence of the aqueous polyurethane
dispersion. This may be effected by adding the vinyl
monomer or monomers to the polyurethane dispersion,
either gradually or all at once, and then subjecting the
- 13 - l 337 3 09
monomer to polymerisation conditions. Alternatively, a
solution of prepolymer in vinyl monomer may be dispersed
in an aqueous medium after which the prepolymer is chain
extended and the vinyl monomer polymerised.
Vinyl monomers which may be polymerised to form
the vinyl polymer component of the aqueous dispersions of
the invention include any radically polymerisable
olefinically unsaturated compounds or mixtures thereof.
Thus, there may be mentioned hydrocarbon monomers, for
example butadiene, isoprene, styrene and divinyl benzene,
acrylic and substituted acrylic monomers, for example
acrylic and methacrylic acids, acrylonitrile, methyl,
ethyl, 2-hydroxyethyl, butyl and isobutyl acrylates and
methacrylates, acrylamide, methacrylamide,
N-methylolacrylamide and other com~o~ly used monomers
such as vinyl esters, vinyl ethers, vinyl ketones and
heterocyclic vinyl compounds.
Polymerisation of the vinyl monomer or monomers
may be effected using conventional emulsion
polymerisation techniques. Thus, the monomer may be
contacted with free radical initiators, especially
initiators partitioned between the aqueous and organic
phases, for example a combination of
t-butylhydroperoxide, isoascorbic acid and Fe.EDTA.
The weight ratio of polyurethane to vinyl polymer
ir. the dispersions of the invention is suitably in the
range from 9:1 to 1:9 with a solid content in the range
from about 30% to about 45% by weight. Viscosities are
usually between 20 and 1000 cps at 25C and the pH is
commonly around 7.5 to 9Ø
The aqueous polymer dispersions of the invention
are stable for long periods of time. They may
advantageously be employed as coating compositions for
which purpose they may be further diluted with water
_ - 14 - 1337309
and/or organic solvents or they may be supplied in more
concentrated form by evaporation of water and/or organic
components of the liquid medium. As coating compositions,
they may be applied to any substrate including wood,
metals, glass, cloth,leather,paper, plastics, foam and
the like by any conventional method including brushing,
dipping, flow coating, spraying and the like. The
compositions may contain other conventional ingredients
including organic solvents,pigments, dyes, emulsifiers,
surfactants, thickeners, heat stabilisers, levelling
agents, anti-coating agents, fillers, sedimentation
inhibitors, W absorbers, antioxidants and the like
introduced at any stage of the production process or
subsequently. It is also possible to include an amount
of an antimony oxide in the dispersions to enhance the
fire retardant properties. The dispersions may also be
used as adhesives for materials such as polypropylene,
polyester, polyurethane,leather and the like or as
binding agents for various particulate materials.
Compared to TDI based urethane-acrylics, the
polymers derived from the dispersion of the invention are
some 13 to 25% harder. In addition, the MDI based
polymers have better solvent resistance towards methyl
ethyl ketone, ethanol, N-methylpyrrolidinone and
isopropanol. Most importantly, the MDI based
urethane-acrylics have better water resistance properties
compared to the TDI based products.
The invention is illustrated but not limited by
the following Examples.
ExamPle 1
PREPARATION OF WATER REDUCIBLE POLYURETHANE
A 1000 ml 4-neck resin flask equipped with thermo-
meter, overhead stirrer and nitrogen was charged with
143 g (0.286 eq.) of polytetramethylene ether glycol of
molecular weight 1000, 20.4 g (0.286 eq.) cyclohexane
- 15 - l 337 309
dimethanol, 28.9 g (0.432 eq.) of dimethylolpropionic
acid, 126 g of N-methylpyrrolidinone and 25 g of methyl
ethyl ketone. The reactor was heated to 60C until all
the dimethylol propionic acid dissolved and was then
cooled to 20C. To the reactor was added 164.2 g
(1.55 eq.) of a mixture containing 96.4 g (0.775 eq.) of
a 77:23 ratio of 4,4':2,4'-diphenylmethane diisocyanate
and 67.4 g (0.775 eq.) of a 80:20 ratio of
2,6:2,4-toluene diisocyanate. The reaction was allowed
to exotherm to 60-70C while cooling over an ice bath.
After the exotherm was completed, the reaction was
warmed to 65C for two hours. The NC0% of the prepolymer
is 4.1~.
A dispersion of the prepolymer was prepared by
feeding 400 g at 40C into 498 g. of deionized water
containing 17.9 g of triethylamine and 5.93 g of
hydrazine. The dispersion temperature was controlled
between 15-25C and was allowed to stir one hour after
the addition of prepolymer was complete. The dispersion
has a pH of 8.0, viscosity of 85cps, and a solids content
of 31%.
PREPARATION OF URETHANE-ACRYLIC DISPERSION
A 500 ml reactor under nitrogen was charged as
follows:
210 g of the polyurethane dispersion, 69 g of distilled
water, o.16 g of triethylene tetramine, 0.64 g of a 1%
solution of Fe-EDTA, 3.4 g of a 3.5% solution of t-butyl
hydroperoxide and 13 g of a vinyl mixture containing
styrene, butyl acrylate, methyl methacrylate and
acrylonitrile having a 45:19:30:6 ratio. The reaction
mixture was warmed to 35C and 4.1 g of a 1% solution of
isoascorbic acid neutralized with triethyl amine was
added. After the reaction exotherm was complete, another
10.3 g of the 3.5% t-butyl hydroperoxide was added,
~ - 16 - l 33 7 3 0~
followed by the slow feed addition of 52 g of more vinyl
monomers. During the vinyl monomer addition, another
12.3 g of 1% isoascorbic acid triethyl amine was added in
ten separate additions. Total time of addition was one
hour. After the addition was complete, the temperature
was raised to 55C for one hour. The final dispersion
has a solid content of 35%, viscosity of 80 cps and a pH
of 8.2.
7-Day Humid Age Test on B-1000 steel: No effect
107-Day Water Immersion Test on B-1000 steel: No effect
Example 2
PREPARATION OF WATER REDUCIBLE POLYURETHANE
~ A polyurethane was prepared as described in
Example 1, except that only TDI was used. The following
amounts were used to prepare the urethane:
Polytetramethylene glycol 143 g
Dimethylolpropionic acid 28.9 g
1,4-cyclohexane dimethanol 20.4
Methyl ethyl ketone 23
M-pyrol 115
Toluene diisocyanate 80/20 131
Hydrazine 7.5
Water 575
Triethyl amine 22.8
The obtained polyurethane dispersion has a pH of
307.9, solid content of 31% and a viscosity of 110 cps.
- 17 - I 33 7309
PREPARATION OF URETHANE-ACRYLIC DISPERSION
A urethane-acrylic dispersion was prepared as
described in Example 1 except that the TDI containing
urethane was used.
7-Day Humid Test on B-1000 steel: Blisters, rust and
peeling.
7-Day Water Immersion Test on B-1000 steel: rust and
pitted.
EXAMPLES 3-5
PREPARATION OF WATER REDUCIBLE POLYURETHANES
Urethane polymers were prepared as in Example 1
except the following amounts were used:
Equivalents EX.3 EX.4 EX.5
Polytetramethylene 0.45 225 225 225
glycol
Dimethylolpropionic 0.55 36.8 36.8 36.8
acid
M-Pyrol 160 160 140
Methyl ethyl ketone 32 32 28
MDI 4,4':2,4' 77:23 1.5 187.5
50:50 1.5 187.5
TDI 1.5 130.5
Hydrazine 0.47 7.5 7.5 7-5
Triethylamine 0.289 29.2 29.2 29.2
Water 844 844 735
PREPARATION OF URETHANE-ACRYLIC DISPERSIONS
Urethane-acrylic dispersions were prepared as in
Example 1 from each of the 3 urethane polymers, using
216 g of polymer together with
- 18 - l 3373 0~
Water 121
Fe/EDTA 1% 0.65
Triethylene tetramine 0.16
Vinyl monomers 13
TBHPO 3.5% 2.0
Isoascorbic acid 1% 2.4
Vinyl monomers 52
TBHPO 11.7
Isoascorbic acid 14.0
EX.3 EX.4 EX.5
Viscosity, cps 800 45 57
Solids % 30 30 30
pH 9 8.5 9
Humid Age
100F 95% R.H
1 day No effect No effect Blistering
7 day Slight Slight Blister-
Whitening Whitening rust
through
The TDI based polymer of Example 5 is clearly
inferior to the MDI based polymers of Examples 3 and 4 in
humidity resistance.
EXAMPLE 6
A simple urethane-acrylic blend is prepared
by mixing the polyurethane from Example 1 with an acrylic
polymer prepared from styrene, butyl acrylate, methyl
methacrylate and acrylonitrile in a monomer ratio of
45:19:30:6. The blended dispersion had a solids content
of 35%, pH of 8.0 and viscosity of 80 cps.
-19- 13373()q
7-Day Humid Age on B-1000 steel: Whitening, rusted
blisters
7-Day Water Immersion Test on B-1000 steel: whitening,
rusted, blisters
The properties of coatings prepared from the
dispersions of the foregoing Examples are displayed in
Table 1.
- 20 - 1 33730~
o rn ~ ~ W Z ~ 3 ~ ~ Q rn D~
~_ . ~ N ~ r~
~- W~ ~ 0 3 ~D P~ ~S O :~
o ~ ~ ~ W W ~ 3 t~ Z 1--~3 3 ~ 3 3 ~ ~
O1. ~ Q.Q 0 ~ ~ rn ~D~ - I ` O 1 -
3 ~ ~ 3P. ~ ~ ~ ~ o ~t ~D ~: 3 ~ - H
Il 11 11 11 11 11 W 5 ~ ~D ~ O ~ C tt 1--~D 1
X -- ~ ~D :t~ O O O 1--~D t~
o rn ~ ~ ~ Z ~D rn o ~n 3 t~ D ~ : O rD Q
tD 1--0 ~ ~J- I æ æ 3 I p) tD 1--I--Q D ~ O
rn ~D 1 `- IS O O ~C ~ D W -n ; ~ 3
o ~ ~ I- rn ~ N O ~ r~ - n 1~-
D ~ ~ W t5 O ~- O 1~ D tD ~ n~n o
rn ~ ~ D ~ rn o o~
tD ~ D ~ 1-- 01 14
~cn ~ o ~ ~ ~
I--~ O ~ D ~D ~: -- ) O
O ~ 3 tt ~ O '- ~D Z
O '~
W 1~ - O
X S~ D3 ~ W
C ~D ~
c.n p~ D ~ 3
- ~ D t~
Q ~ ~
~ ~ C
o ~3
' 3 ~
W
X c
~ .P Z r~ z: z z z 1~
`~ W . ~ . O ~D O a~ ~1 w o o o o t~ -
W W WWW
~- - - Z
W
o
W
X
~ W W W Z W W W ~n ~ IW Q
O C~ C~ ~ O o~ r~
~ ~ ~ W ~ ~d
W
~ ~a
o
W
X
z z z æ z z ~ IQ
~ W W W W W ~D O a~ n o o o o ~D W
.. ... ww
W tD r~ Z W W ~~ I~ ~ ~ ~ 1
` ` I~ ` ` ~D ~n CD O ~ O O O ~ O ~D
W ~ ~d .
rn Z Z Z Z Z ~ IW
1-- ~D 0~ 0 .P ~1 P O ~D ~ O ~D W
WW WWW -
.. ... ww
- 21 - l 33730q
Example 7 (Comparative Example)
A polyurethane was prepared as described in
Example 1, except that isophorone diisocyanate was used
in place of 2,4':4,4'-MDI. The following amounts were
used to prepare the urethane:
Polytetramethylene glycol (mw = lG00) 143
Dimethylolpropionic acid 28.9
1,4-Cyclohexane dimethanol 20.4
Methyl et~yl Ketone 25.4
N-methyl pyrrolidone 127.4
Toluene diisocyanate 80/20 67.4
Isophorone diisocyanate 97.0
N 2 H 4 9 . 8
H2O 575
Triethylamine 22.8
The obtained dispersion has a pH of 8.47 and a
viscosity of 2650 cps at 31% solids.
PREPARATION OF URETHANE-ACRYLIC DISPERSION
A urethane-acrylic dispersion was prepared as
described in Example 1 except that the TDI-IPDI
containing urethane was used.
7-day Humid Age Test on B-1000 steel: blisters,
rust whitening and peeling.
7-day Water Immersion Test on B-1000 steel: rust,
blisters and pitted.
Example 8 (Comparative Example)
A polyurethane was prepared as described in
Example 1, except that methane dicyclohexyl diisocyanate
was used in place of 2,4':4,4'-MDI. The following amounts
were used to prepare the urethane:
Polytetramethylene glycol (mw = 1000) 143
Dimethylolpropionic acid 28.9
1,4-Cyclohexane dimethanol 20.4
Methyl ethyl Ketone 25.4
N-Methyl pyrrolidone 127.4
_ - 22 - 1 33 7 3 09
Toluene diisocyanate 80/20 67.4
Methane dicyclohexyldiisocyanate 97
N2H~ 7.8
H2O 575
Triethylamine 22.8
The obtained dispersion has a pH of 7.9, a
viscosity of 90 cps and a solids content of 31%.
PREPARATION OF URETHANE-ACRYLIC DISPERSION
A urethane-acrylic dispersion was prepared as
described in Example 1 except that the TDI-methane
dicyclohexane diisocyanate was used.
7-day Humid Age Test on B-1000 steel: blisters,
whitening, rust and peeling.
7-day Water Immersion Test on B-1000 steel:
blisters, rust and peeling.
